PARCUS MEDICAL LLC BIOCOMPOSITE SUTURE ANCHORS (SCREW-IN); FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
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Catalog Number 11126T |
Device Problem
Break (1069)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/28/2024 |
Event Type
malfunction
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Event Description
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This report is being submitted in pursuant to the provisions of 21 cfr, part 803.This report does not reflect a conclusion by parcus or its employees that the report constitutes an admission that the device, parcus, or its employees caused or contributed to a potential patient event documented on this report.On 02april2024 it was reported to parcus that during a rotator cuff shoulder procedure on a patient of unknown age and demographic, the anchor broke upon insertion into the patient's bone.There was no negative patient reaction reported.There was no delay in the procedure reported.There was no defect of the device or packaging prior to use of the device.The current status of the patient is unknown.Additional information was solicited.
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Manufacturer Narrative
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This complaint is still under investigation.A supplemental report will be submitted upon receipt of new and relevant information or upon completion of the investigation by the manufacturing plant.
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Event Description
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This report is being submitted in pursuant to the provisions of 21 cfr, part 803.This report does not reflect a conclusion by parcus or its employees that the report constitutes an admission that the device, parcus, or its employees caused or contributed to a potential patient event documented on this report.On 02april2024 it was reported to parcus that during a rotator cuff shoulder procedure on a patient of unknown age and demographic, the anchor broke upon insertion into the patient's bone.There was no negative patient reaction reported.There was no delay in the procedure reported.There was no defect of the device or packaging prior to use of the device.The current status of the patient is unknown.Additional information was solicited.
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Manufacturer Narrative
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This complaint is still under investigation.A supplemental report will be submitted upon receipt of new and relevant information or upon completion of the investigation by the manufacturing plant.Supplemental report: the reported event is not confirmed.Additional information was not provided upon request.The device was not available for analysis.The batch record was reviewed.There was no nonconformances related to the reported event in the batch record.The product was manufactured and released to applicable procedures and specifications.A three year retrospective review of all nonconformances was performed.There was no nonconformances for this part number.The reported event will continue to be monitored and trended for future analysis.A supplemental report will be submitted upon receipt of new and relevant information.
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Search Alerts/Recalls
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